Fig. 1: Mutation-specific mechanism of ASXL1 c.1934dupG detection using the 9G primer
From: ASXL1 c.1934dup;p.Gly646Trpfs*12—a true somatic alteration requiring a new approach
A ASXL1 c.1934dupG (9G repeat)—primer and template complementary. B Wild-type (8G repeat)—primer and template partially mismatched. Resulting PCR product amplification characteristics constitute signal
